NDC 51435-001 Neutracett Ulcer

NDC Product Code 51435-001

NDC 51435-001-01

Package Description: 28.3 g in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Neutracett Ulcer with NDC 51435-001 is product labeled by Advanced Biomedics Inc. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates multiple concept unique identifiers (RXCUI) are associated with this product:

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • PPG-5-CETETH-20 (UNII: 4AAN25P8P4)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Advanced Biomedics Inc
Labeler Code: 51435
Start Marketing Date: 05-28-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Neutracett Ulcer Product Label Images

Neutracett Ulcer Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Inactive Ingredient

Inactive Ingredients: Water (Aqua), Neutracett Complex (Hyaluronic
Acid, DL Panthenol), PPG-5-Ceteth-20, Ammonium Acryloyldimethyltaurate/VP
Copolymer, Phenoxyethanol, Chlorphenesin, Benzoic Acid.

Otc - Active Ingredient

Active ingredients/PurposeAllantoin 0.5%   Skin ProtectantGlycerin 5.0%   Skin Protectant

Otc - Ask Doctor

Ask a doctor before use if you have: *serious burns *
deep or puncture wounds * animal bitesQuestions? 800-833-4164www.neutracett.com Patents

Otc - Do Not Use

Do not use: *if you are allergic to any of the
ingredients *avoid contact with the eyes

Otc - Stop Use

Stop use and ask a doctor: * if condition worsens or does not improve
after 7 days * if rash or other allergic reactions occur

Otc - Purpose

Uses: Helps protect the skin so your body can heal minor wounds
including diabetic, pressure and other ulcers.


Warnings: For external use only.

Dosage & Administration

Directions: Gently clean area with mild cleanser. Apply gel directly on
ulcer 2-3 times per day or as directed. May be covered with sterile bandage.
See website for more information.

* Please review the disclaimer below.